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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827166Generated: October 29, 2026

Triethylamine → Benzyl 4-{[(5-fluoro-pyrimidin-2-yl)amino]methyl}piperidine-1-carboxylate

https://huagongshe.com/reaction/1827166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-5-fluoropyrimidineHCID 583466—
Reactant4-Aminomethyl-1-N-Cbz-piperidineHCID 21955499—
SolventDimethylformamideHCID 6228—
ProductBenzyl 4-{[(5-fluoro-pyrimidin-2-yl)amino]methyl}piperidine-1-carboxylateHCID 10132254—

Reaction Steps

A solution of benzyl-4-(aminomethyl)piperidine-1-carboxylate (EXAMPLE 13, Step 1, 0.10 g, 0.40 mmol), 2-chloro-5-fluoro-pyrimidine (0.053 g, 0.40 mmol) and triethylamine (0.11 mL, 0.81 mmol) in DMF (0.5 mL) was heated at 100° C. for 6 h, then concentrated in vacuo. The residue was purified by silica gel chromatography (10 CH2Cl2:1-20 IPA:89-70 hexane) to give 4-[(5-fluoro-pyrimidin-2-ylamino)-methyl]-piperidine-1-carboxylic acid benzyl ester. M.S.(M+1):345.29

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053089B2
Source datasetuspto-grants-2006_05
ORD IDord-e80c997706f74c53abf1f93f6ec3f25b
Source noteuspto-grants-2006_05